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Expression of cutaneous immunity markers during infant skin maturation

机译:皮肤病患者皮肤成熟期间的表达

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Abstract Background/Objectives Infant skin undergoes a maturation process during the early years of life. Little is known about the skin's innate immunity. We investigated the dynamics of innate immunity markers collected from the surface of infant skin during the first 36 months of life. Methods A total of 117 healthy infants aged 3‐36 months participated in the study. We extracted human beta defensin‐1 and interleukin 1 alpha and its receptor antagonist using transdermal analysis patches from the skin surface of the posterior lower leg area. The extracts were analyzed using a spot enzyme‐linked immunosorbent assay. Results Skin surface human beta defensin‐1 levels were higher early in life and decreased with infant age. The ratio of interleukin 1 alpha receptor antagonist to interleukin 1 alpha did not change significantly with age but showed a distinct difference between sexes, with female infants having higher values than male infants. Conclusion As is the case with skin structure and functional properties, cutaneous innate immunity also appears to undergo a maturation period during infancy, with innate immunity slowly declining as adaptive immunity takes over. Sex differences in immune markers may explain sex‐dependent susceptibilities to infection.
机译:抽象背景/目标婴儿皮肤在生命的早期进行成熟过程。对皮肤的先天免疫感到难以知。我们调查了在生命的前36个月内从婴儿皮肤表面收集的先天免疫标记的动态。方法参加了3-36个月的117岁的健康婴儿参加了这项研究。使用从后部腿部的皮肤表面的透皮分析贴片提取人β防御蛋白-1和白细胞介素1α及其受体拮抗剂。使用斑点酶联免疫吸附测定分析提取物。结果皮肤表面人β防御素-1水平较早较高,婴幼儿较高。白细胞介素1α受体拮抗剂与白细胞介素1α的比例随着年龄而显着变化,但表现出性别不同的差异,具有比男性婴儿更高的母婴。结论与皮肤结构和功能性质的情况如此,皮肤先天免疫也似乎在婴儿期间发生成熟时期,随着自适应免疫接管,先天免疫慢慢下降。免疫标志物的性差异可以解释对感染的性依赖性敏感性。

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